Wang Fengmei, Ju Lin, Wu Binglan, Li Shuhui, Peng Jian, Chen Yetao, Getaye Sendeku Marshet, Wang Kairui, Cai Yuchen, Yi Jun, Yang Ying, Wang Zhenxing, Sun Xiaoming
State Key Laboratory of Chemical Resource Engineering, College of Chemistry, Beijing University of Chemical Technology, Beijing, 100029, P. R. China.
CAS Key Laboratory of Nanosystem and Hierarchical Fabrication, National Center for Nanoscience and Technology, Beijing, 100029, P. R. China.
Angew Chem Int Ed Engl. 2024 Apr 24;63(18):e202402033. doi: 10.1002/anie.202402033. Epub 2024 Mar 12.
Heterogeneous electrocatalysis closely relies on the electronic structure of the catalytic materials. The ferroelectric-to-paraelectric phase transition of the materials also involves a change in the state of electrons that could impact the electrocatalytic activity, but such correlation remains unexplored. Here, we demonstrate experimentally and theoretically that the intrinsic electrocatalytic activity could be regulated as exampled by hydrogen evolution reaction catalysis over two-dimensional ferroelectric CuInPS. The obvious discontinuity in the overpotential and apparent activation energy values for CuInPS electrode are illustrated during the ferroelectric-to-paraelectric phase transition caused by copper displacement around T point (318 K), revealing the ferroelectro-catalytic effect on thermodynamics and kinetics of electrocatalysis. When loading Pt single atom on the CuInPS, the paraelectric phase one showed an improved hydrogen evolution activity with smaller apparent activation energy over the ferroelectric phase counterpart. This is attributed to the copper hopping between two sulfur planes, which alternate between strong and weak H adsorption at the Pt sites to simultaneously promote H reactant adsorption and H product desorption.
多相电催化紧密依赖于催化材料的电子结构。材料从铁电相到顺电相的转变也涉及电子状态的变化,这可能会影响电催化活性,但这种相关性仍未得到探索。在此,我们通过实验和理论证明,二维铁电体CuInPS上的析氢反应催化为例,本征电催化活性是可以调控的。在T点(318 K)附近由于铜的位移导致的从铁电相到顺电相转变过程中,CuInPS电极的过电位和表观活化能值出现明显的不连续性,揭示了铁电催化对电催化热力学和动力学的影响。当在CuInPS上负载Pt单原子时,顺电相的析氢活性相较于铁电相有所提高,表观活化能更小。这归因于铜在两个硫平面之间的跳跃,其在Pt位点上的H吸附强弱交替,从而同时促进H反应物的吸附和H产物的脱附。